EP2611750A2 - Temperable three layer antireflective coating, coated article including temperable three layer antireflective coating, and/or method of making the same - Google Patents
Temperable three layer antireflective coating, coated article including temperable three layer antireflective coating, and/or method of making the sameInfo
- Publication number
- EP2611750A2 EP2611750A2 EP11728083.4A EP11728083A EP2611750A2 EP 2611750 A2 EP2611750 A2 EP 2611750A2 EP 11728083 A EP11728083 A EP 11728083A EP 2611750 A2 EP2611750 A2 EP 2611750A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- index layer
- coated article
- coating
- medium
- index
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000006117 anti-reflective coating Substances 0.000 title claims description 29
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000000576 coating method Methods 0.000 claims abstract description 123
- 239000011248 coating agent Substances 0.000 claims abstract description 103
- 239000000758 substrate Substances 0.000 claims abstract description 52
- 239000011521 glass Substances 0.000 claims abstract description 40
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 18
- 239000010703 silicon Substances 0.000 claims abstract description 18
- 238000010438 heat treatment Methods 0.000 claims description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 22
- 230000005540 biological transmission Effects 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 10
- 229910052742 iron Inorganic materials 0.000 claims description 8
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 6
- 239000010936 titanium Substances 0.000 claims 6
- 229910052719 titanium Inorganic materials 0.000 claims 6
- 230000003287 optical effect Effects 0.000 abstract description 13
- 229910020286 SiOxNy Inorganic materials 0.000 abstract description 10
- 239000000126 substance Substances 0.000 abstract description 3
- 239000010410 layer Substances 0.000 description 180
- 230000003667 anti-reflective effect Effects 0.000 description 66
- 238000005496 tempering Methods 0.000 description 32
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 21
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 19
- 239000000463 material Substances 0.000 description 16
- 229910003087 TiOx Inorganic materials 0.000 description 7
- HLLICFJUWSZHRJ-UHFFFAOYSA-N tioxidazole Chemical compound CCCOC1=CC=C2N=C(NC(=O)OC)SC2=C1 HLLICFJUWSZHRJ-UHFFFAOYSA-N 0.000 description 7
- 230000008859 change Effects 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000002310 reflectometry Methods 0.000 description 5
- 238000005336 cracking Methods 0.000 description 4
- 239000008186 active pharmaceutical agent Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000004767 nitrides Chemical class 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- 229910000906 Bronze Inorganic materials 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010974 bronze Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000005329 float glass Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000005346 heat strengthened glass Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 102220047090 rs6152 Human genes 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- HUAUNKAZQWMVFY-UHFFFAOYSA-M sodium;oxocalcium;hydroxide Chemical compound [OH-].[Na+].[Ca]=O HUAUNKAZQWMVFY-UHFFFAOYSA-M 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000005341 toughened glass Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
- G02B1/11—Anti-reflection coatings
- G02B1/113—Anti-reflection coatings using inorganic layer materials only
- G02B1/115—Multilayers
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/3411—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions with at least two coatings of inorganic materials
- C03C17/3429—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions with at least two coatings of inorganic materials at least one of the coatings being a non-oxide coating
- C03C17/3435—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions with at least two coatings of inorganic materials at least one of the coatings being a non-oxide coating comprising a nitride, oxynitride, boronitride or carbonitride
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2217/00—Coatings on glass
- C03C2217/70—Properties of coatings
- C03C2217/73—Anti-reflective coatings with specific characteristics
- C03C2217/734—Anti-reflective coatings with specific characteristics comprising an alternation of high and low refractive indexes
Definitions
- a temperable antireflective (AR) coating utilizes SiO x N y as the medium index layer of the coating.
- the coating may include the following layers from the glass substrate outwardly: silicon oxynitride (e.g., SiO x N y ) as the medium index layer/titanium oxide (e.g., TiOx) as the high index layer/silicon oxide (e.g., SiOx) as the low index layer.
- the thicknesses and types of stress in each layer may be optimized in order to produce a temperable, three layer antireflective coating.
- Antireflective (AR) coatings are known in the art.
- AR coatings in the visible range are widely used on glass in electronics, lighting, appliances, architectural, and display applications.
- tempered or heat-strengthened glass may be required. Tempering or heat strengthening of the glass is sometimes done prior to the deposition of the AR coating to avoid unwanted changes in the optical, mechanical, or aesthetic quality of the coating as a consequence of exposing the coating to the high temperatures required for tempering and other forms of heat treatment.
- this "temper then coat” method may be undesirable in certain circumstances.
- a coated article comprising an antireflective coating supported by a major surface of a substrate, the substrate being heat treated together with the antireflective coating, wherein the antireflective coating comprises, in order moving away from the substrate: a medium index layer comprising silicon oxynitride and having a index of refraction of from about 1.65 to 2.0 at 380 nm, 550 nm, and 780 nm wavelengths, a high index layer having an index of refraction of at least about 2.0 at 380 nm, 550 nm, and 780 nm wavelengths, and a low index layer having an index of refraction of from about 1.4 to 1.6 at 380 nm, 550 nm, and 780 nm wavelengths, wherein the medium index layer has compressive residual stress after heat treatment.
- a heat treatable coated article comprising: an antireflective coating supported by a major surface of a substrate, wherein the antireflective coating comprises, in order moving away from the substrate: a medium index layer comprising silicon oxynitride and having a index of refraction of from about 1.65 to 2.0 at 380 nm, 550 nm, and 780 nm wavelengths, a high index layer having an index of refraction higher than that of the medium index layer at 380 nm, 550 nm, and 780 nm wavelengths., and a low index layer having an index of refraction lower than that of the medium index layer at 380 nm, 550 nm, and 780 nm wavelengths, wherein the medium index layer and the low index layer have compressive residual stress after any heat treatment, the high index layer has tensile residual stress after any heat treatment, and the antireflective coating has a net compressive residual stress.
- a heat treatable coated article comprising an antireflective coating supported by a major surface of a substrate, wherein the antireflective coating comprises, in order moving away from the substrate: a medium index silicon-inclusive layer having a index of refraction of 1.8 or less 550 nm and 780 nm wavelengths and 2.0 or less at 380 nm, a high index layer having an index of refraction higher than that of the medium index layer at 380 nm, 550 nm, and 780 nm wavelengths, wherein the high index layer has a thickness no greater than about 20 nm, and a low index layer having an index of refraction lower than that of the medium index layer at 380 nm, 550 nm, and 780 nm wavelengths, wherein the medium index layer and the low index layer have compressive residual stress, the high index layer has tensile residual stress, and the antireflective coating has a net compressive residual stress
- a method of making a coated article with a three-layered antireflection coating comprising: disposing a medium index layer, directly or indirectly, on a glass substrate; disposing a high index layer over and contacting the medium index layer; disposing a low index layer over and contacting the high index layer; and heat-treating the glass substrate with the antireflective coating thereon, and wherein the coated article has a net compressive residual stress.
- FIGURE 1 is an example of a three-layered temperable AR coating generally according to certain example embodiments of this invention.
- FIGURE 2 is an example of an optimal three-layered temperable AR coating made according to certain example embodiments of this invention.
- FIGURE 3 is an example of a two-sided temperable AR coating made according to certain example embodiments of this invention.
- FIGURE 4 is a graph of the first surface reflectivity comparison of an AR coating before and after exposure to a tempering environment.
- FIGURE 5 is a graph showing changes in the reflectivity between the as-deposited and tempered states compared to the tristimulus values used in the color calculations.
- FIGURE 6 is a table showing the as-coated visible transmission and color characteristics of an AR coating made according to certain example embodiments of this invention.
- FIGURE 7 is a table showing the resulting optical qualities of an AR coating made according to certain example embodiments of this invention after exposure to 650 degrees C for 10 minutes.
- FIGURE 8 is a table showing examples of the compressive and tensile stresses than can arise in different layers, both as-deposited and after heat- treatment and/or tempering.
- FIGURE 9 is a graph showing the residual stress for coatings with various titanium oxide thicknesses.
- FIGURE 10 is a graph comparing the light transmission of a coated article made according to examples described herein, before and after exposure to a tempering environment.
- FIGURE 1 1 is a table showing example optimal thicknesses and refractive indices for AR coatings made according to certain example
- Certain example embodiments of this invention relate to a coated article including an antireflective coating, and/or a method of making the same.
- a temperable antireflective (AR) coating is provided.
- AR coatings in the visible range are widely used on glass in electronics, lighting, appliances, architectural, and display applications.
- tempering or heat strengthening of the glass is sometimes done prior to the deposition of the AR coating to avoid unwanted changes in the optical, mechanical, or aesthetic quality of the coating as a consequence of exposing the coating to the high temperatures required for tempering and other forms of heat treatment, there are drawbacks associated with the "temper then coat" method under certain example circumstances.
- tempering prior to coating may be undesirable for large area coaters.
- the final size of the tempered/heat treated substrate to be coated may be of a dimension that does not efficiently employ the large area coating capability, which is useful when attempting to increase achieve the high efficiencies possible by virtue of high volume glass coating manufacturing techniques.
- a three- layered antireflective coating that can be tempered and/or heat treated while preserving its aesthetic quality and high chemical and mechanical durability after exposure to temperatures typically encountered in tempering and/or heat treating environments would be advantageous.
- Existing three layer AR coatings may not be sufficiently temperable in certain example embodiments, e.g., in the sense that such coatings may not survive the tempering process in a usable or desirable form.
- some materials utilized in AR coatings may have high tensile residual stress after exposure to temperatures greater than, for example, 300 degrees C.
- the tensile residual stress of one layer When the tensile residual stress of one layer is so high such that it results in a net tensile stress in the multilayer stack, this stress may be sufficient to cause an aesthetic degradation of the coating. This and/or similar problems may, for example, result in the cracking of the coating. Therefore, it may be advantageous to reduce the tensile residual stress in a layer in an AR coating, offset the tensile residual stress by reducing the thickness of that layer, balance the tensile residual stress in one layer with compressive residual stress in the other layer(s), etc.
- Compressive stress when applied, acts toward the center of a material.
- compressive stress acts toward the center of a material.
- tensile stress acts toward the center of a material.
- the material when a material is subjected to compressive stress, the material is under compression.
- tensile stress on the other hand, the material may suffer stretching or elongation. Accordingly, if too much tensile residual stress is present in a layer in a coating, the layer and/or coating may suffer deformation or cracking in certain instances. Therefore, in certain example embodiments, it may be more desirable for a coating to have a net compressive residual stress rather than a net tensile residual stress.
- Fig. 1 is a cross sectional view of an example coated article according to an example embodiment of this invention.
- the coated article of the Fig. 1 embodiment includes substrate 1 that supports temperable antireflective (AR) coating 3.
- Substrate 1 is typically a glass substrate (e.g., clear, green, bronze, or blue-green glass substrate from about 1.0 to 10.0 mm thick), but may be other materials in certain example instances such as polycarbonate or acrylic.
- the AR coating 3 includes medium index layer 5, high index layer 7, and low index layer 9.
- the medium, high, and low index layers 5, 7, and 9 may be provided in this order moving away from the substrate 1 in certain example embodiments of this invention.
- the layers may directly contact one another.
- the low index layer 9 is the outermost layer of the coating 3, whereas the medium index layer 5 is the bottom-most layer of the AR coating 3.
- the AR coating 3 is a dielectric type coating in that each of layers 5, 7 and 9 is a dielectric layer (i.e., not electrically conductive).
- the AR coating 3 of the Fig. 1 example embodiment has no IR reflecting layer (i.e., no metallic layer of Ag, Au, or the like), and no transparent conductive oxide (TCO) layer such as a pyrolytically deposited metal
- low-E coatings may be used in connection with different embodiments of this invention, e.g., in combination with the AR coating 3 on the same or opposite side of the substrate 1.
- a temperable AR coating includes at least three dielectric layers, namely a high index layer, a medium index layer and a low index layer.
- the meanings of "high”, “medium” and “low” are simply that the medium index layer has an index of refraction (n) less than that of the high index layer and greater than that of the low index layer (e.g., no specific values are required merely by the use of "high”, “medium” and “low”).
- the high, medium, and low index layers are typically dielectric layers in certain example embodiments of this invention, in that they are not electrically conductive.
- the refractive index (n) of medium index layer 5 is less than the refractive index of the high index layer 7 and greater than the refractive index of the low index layer 9.
- the low index layer 9 may be of or include silicon or an oxide thereof (e.g., SiO 2 or other suitable
- the high index layer 7 may be of or include a metal oxide, metal nitride and/or metal oxynitride such as titanium oxide (e.g., Ti0 2 or other suitable stoichiometry), zinc oxide, silicon or a nitride thereof, or the like.
- a metal oxide, metal nitride and/or metal oxynitride such as titanium oxide (e.g., Ti0 2 or other suitable stoichiometry), zinc oxide, silicon or a nitride thereof, or the like.
- the AR coating of Fig. 2 is the same as the AR coating of Fig. 1 , but instead shows example materials used for each of the medium, high, and low index layers.
- the medium index layer 5 is a bottom layer of the AR coating and has an index of refraction (n) of from about 1.60 to 2.0, more preferably from about 1.65 to 1.9, even more preferably from about 1.7 to 1.8, and most preferably from about 1.7 to 1.79 (at 550 nm).
- an ideal refractive index of medium index layer 5 is from about 1.8 to 2.0.
- the index of refraction of medium index layer 5 is from about 1.65-1.8 at 780 nm.
- medium index layer 5 have desired optical and mechanical properties in the as-deposited state as well as after exposure to temperatures typical in tempering and/or heat treating environments. It will be appreciated that materials such as aluminum oxynitride, though having desired properties in the as-deposited state, may degrade in optical and/or mechanical properties after exposure to temperatures typical in tempering and/or heat treating environments. Aluminum oxynitride may, however, be used in different embodiments of this invention if it can be made to be sufficiently survivable.
- the medium index layer 5 has a compressive residual stress in both the as-coated and heat-treated states.
- this compressive residual stress may help to offset the tensile residual stress in the other layer(s) in the stack. In certain instances, this may promote a net compressive stress in the three layer AR stack, which discourages cracking of the coating during the tempering and/or heat treating processes.
- Medium index layer 5 preferably has a thickness of from about 75 to
- silicon oxynitride e.g., SiOxNy
- silicon oxynitride can be deposited to have an index of refraction of from about 1.60 to 2.0, more preferably from about 1.65 to 1.9, even more preferably from about 1.7 to 1.85 or 1.7 to 1.8, and most preferably from about 1.7 to 1.79 (at 550 nm), and will not significantly degrade in its mechanical or optical properties upon tempering and/or heat treatment.
- a layer of or comprising silicon oxynitride e.g., SiOxNy
- the high index layer 7 is provided over the medium index layer 5of the AR coating 3.
- Layer 7 has an index of refraction of at least about 2.0, preferably from about 2.1 to 2.7, more preferably from about 2.25 to 2.55, and most preferably from about 2.3 to 2.5 (at 550 nm) in certain example embodiments.
- an ideal index of refraction of high index layer 7 at 380 nm may be from about 2.7 to 2.9 (and all subranges therebetween). In further example embodiments, an ideal index of refraction of high index layer 7 at 780 nm may be from about 2.2 to 2.4 (and all subranges therebetween). [0035] High index layer 7 preferably has a thickness of from about 5 to 50 nm, more preferably from about 10 to 35 nm, even more preferably from about 12 to 22 nm, and most preferably from about 15 to 22 nm. In certain exemplary embodiments, the high index layer 7 has a thickness of less than about 25 nm.
- titanium oxide e.g., TiOx
- titanium oxide has a high tensile residual stress after exposure to temperatures above 300 degrees C.
- the high tensile stress in this layer is associated with a phase change from amorphous to crystalline, observed between the as-coated and as-heat treated states. This phase change, in certain instances, occurs at a temperature below the maximum temperature of exposure of the coating during a typical tempering and/or heat treating process.
- the greater the thickness of the titanium oxide-based layer the greater the tensile residual stress.
- the high tensile residual stress in the titanium oxide-based layer can case an overall large net tensile stress in the three layer stack.
- temperable AR coating including a high index layer of or including titanium oxide comprises other layers (e.g., medium index layer and/or low index layer) having and/or promoting net compressive residual stress after tempering and/or heat treating, in order to offset the high tensile stress of titanium oxide based layer after exposure to high temperatures.
- the physical thickness of the high index titanium oxide-based layer 7 e.g., TiOx
- this will advantageously reduce the net tensile stress of the layer, and may promote a net compressive residual stress for the overall coating.
- the physical thickness of the titanium oxide-based layer is limited, and the other layers are of materials having compressive residual stresses after tempering and/or heat treatment, it has surprisingly been found that a chemically and mechanically durable tempered coated article with good antireflective properties can be achieved.
- the low index layer 9 is provided over the high index layer 7 of the AR coating 3.
- Layer 9 has an index of refraction of from about 1.4 to 1.6, more preferably from about 1.45 to 1.55, and most preferably from about 1.48 to 1.52 (at 550 nm) in certain example embodiments.
- an ideal index of refraction of low index layer 9 at 380 nm may be from about 1.48 to 1.52 (and all subranges therebetween).
- an ideal index of refraction of low index layer 9 at 780 nm may be from about 1.46 to 1.5 (and all subranges therebetween).
- low index layer 9 has a thickness of from about 70 to 130 nm, more preferably from about 80 to 120 nm, even more preferably from about 89 to 109 nm, and most preferably from about 100 to 1 10 nm.
- low index layer 9 have an index of refraction lower than both the medium and high index layers, and in certain example embodiments, the refractive index of low index layer 9 may be less than that of the glass substrate upon which the coating is provided.
- An example material for use as a low index layer is silicon oxide (e.g., SiOx).
- silicon oxide e.g., SiOx
- the use of silicon oxide (e.g., SiOx) as the low index layer in a temperable three layer AR coating in certain example embodiments is
- a low index layer based on silicon oxide advantageously has a compressive residual stress in both the as-coated and heat-treated/tempered states.
- the compressive residual stress in a low index layer based on silicon oxide may help to offset the tensile residual stress in the titanium oxide-based layer. Utilizing a low index layer with compressive residual stress in conjunction with a high index layer with high tensile residual stress helps to promote a net compressive stress in a temperable three layer AR stack in certain example embodiments. This is advantageous in that it may help discourage cracking of the AR coating 3 during tempering and/or heat treating the coated article in certain example embodiments.
- the AR coating 3 of Figs. 1 and 2 may be provided on only one major surface of glass substrate 1 as shown in Figs. 1 and 2.
- Fig. 3 illustrates an example embodiment of this invention where the coating 3 is provided on both the major surfaces of the glass substrate 1.
- a first AR coating 3 is provided on a first major surface of the substrate 1
- a second AR coating 3 is provided on a second major surface of the substrate 1.
- the temperable AR coating may be designed to reduce undesired reflection. In most cases, reduced reflection comes with increased transmission such as AR on picture frame glass that a higher than 98% transmission is desired. However, the increased transmission may not always be desired. For example, the AR coating in the area overlapped with black matrix in a display would benefit from a reflectivity that is as low as possible, but transmission (T) is relatively unimportant. In other words, as will be appreciated by those skilled in the art, the transmission depends at least in part on the substrates and/or applications.
- Coated articles with antireflection coatings 3 are useful in certain window applications as mentioned herein.
- coated articles according to certain example embodiments of this invention may have a visible transmission of at least about 50%, more preferably of at least about 60%, and most preferably of at least about 70%.
- Such windows may be monolithic window glazings, insulating glass (IG) units, vacuum insulating glass (VIG) units, and/or the like.
- IG and/ or VIG example applications the one or more substrates may support the antireflective coating 3 as shown and described herein.
- Example 1 An example AR coating 3 was made as follows:
- SiO x N y layer 5 (medium index layer) about 95 nm thick, Ti0 2 layer 7 (example high index layer) about 21 nm thick, and SiO 2 layer 9 (example low index layer) about 105 nm thick.
- the clear glass substrate was about 5 mm thick, and was soda lime silica type glass.
- Each of layers 5, 7, and 9 was deposited on the glass substrate 1 by sputtering a target(s).
- the coating 3 was provided on only one major surface of the glass substrate in certain instances as shown in Fig. 1, but may be provided on both major surfaces of the glass substrate in other instances as shown in Fig. 3.
- the coating was tempered at 650 degrees C for 10 minutes.
- Fig. 4 is a graph showing a comparison of the first surface
- Fig. 4 illustrates the reflection spectra of an example having SiOxNy adjusted to achieve a refractive index for the medium index layer 5 of from about 1.7-1.8 (at 550 nm), on one major surface of the glass substrate. It can be seen that excellent AR characteristics (e.g., low R%) are achieved in a wavelength range of from about 450 to 650 ran, and even more so from about 500 to 600 ran. The design minimizes or reduces photopic reflection (CIE-C, 2°), and the measured value was less than 0.4%.
- the coated article has a photopic reflection of less than about 3.0%, more preferably less than about 1.0%, more preferably less than about 0.5%, and most preferably less than about 0.25%.
- AR R tempered - R as-coated
- the largest changes in the reflectivity occur in regions where the tristimulus values are close to zero. This results in a reduced amount of change in the reflected color between the as-coated and tempered/heat-treated states. This consideration is independent of the source illuminant.
- Fig. 6 is a table showing the as-coated visible reflection, visible transmission, and color values at normal incidence (111. 2°C) (with backside reflection).
- Fig. 7 is a table showing the resulting optical quantities of the samples in Fig. 6 after exposure to 650 degrees C for 10 minutes.
- Figs. 6 and 7 can be used to compare the change in the optical quantities indicated between the as-coated and heat-treated/tempered states.
- the optical quantities shown are for three substantially equally spaced cross-coater positions (P,C,V) across a total width of 96 inches.
- P,C,V substantially equally spaced cross-coater positions
- the number of coater positions, their locations, and/or the total width may vary in different embodiments of this invention.
- Fig. 8 is a table showing additional data regarding the stress in certain example embodiments of a three-layer temperable AR coating.
- Fig. 8 contains information about a coating made in a similar manner to Example 1 , as well as comparative examples, but does not necessarily reflect information from Example 1 itself.
- the first coating (a) in Fig. 8 is a three-layer AR coating made according to certain example embodiments of this invention, and gives the values and types of the net residual stress in the coating as-deposited, and after heat- treating and/or tempering at 650 degrees C for 10 minutes.
- the negative values for ⁇ ⁇ and o y are indicative of the stress being compressive.
- Positive values indicate tensile stress.
- coatings (a), (b), and (c) it can be seen that the as-deposited net residual stress values are all negative. Therefore, as- deposited, each of these coatings has a net compressive residual stress. However, upon heat-treating and/or tempering, the stress in these coatings moves more toward tensile residual stress. As can be seen from Fig. 8, coating (a)'s titanium oxide-based layer has a thickness of 19 nm. Because the compressive residual stress of the silicon oxide and silicon oxynitride-based layers is higher than the tensile residual stress of the titanium oxide-based layer, the net residual stress of coating (a), even after heat-treatment, is compressive rather than tensile.
- this net compressive stress will result in a more durable coating (as compared to a coating with a net tensile stress).
- Comparative coatings (b) and (c) show that when the titanium oxide-based layer is thicker - 100 nm in coating (b) and 102 nm in coating (c), after heat-treating, the net residual stress is tensile (demonstrated by the positive ⁇ ⁇ and o y . values).
- the stress values for single layers (i) and (ii) are provided simply to show that the residual stress of both a silicon oxide-based layer and a silicon oxynitride-based layer is compressive both before and after heat treating. These compressive residual stress values each act to offset the tensile residual stress of the titanium oxide-based layer.
- a temperable three-layered AR coating that maintains durability even after heat-treatment may be produced, in certain example embodiments, by ( 1) including layer(s) having a compressive residual stress, e.g., low index layers such as silicon oxide and medium index layers such as silicon oxynitride, and/or (2) modifying layers prone to having tensile stress, such as high index titanium oxide-based layer(s), e.g., by reducing their thickness to less than about 25 nm (more preferably less than about 22 nm, and even more preferably approximately equal to or less than 20 nm).
- layers having a net compressive stress may be made by other means.
- Fig. 9 is a graph comparing the as-deposited stress and stress after heating in for coatings (a) and (b) from Fig. 8.
- Fig. 9 shows that coating (a) has compressive residual stress both before and after heating.
- Fig. 9 also shows that coating (b) (a comparative -example including a titanium oxide-based layer having a thickness of 100 nm) has a net compressive stress prior to heating; however, after heat treating, coating (b) has a net tensile stress.
- reducing the amount of tensile stress present in an overall coating can help improve the durability of the coating.
- Example 2 A temperable AR coating was applied to both surfaces of a glass substrate (e.g., a double sided coating was made).
- the double-sided coating (as shown in Fig. 3) also maintains its optical and aesthetic qualities after tempering/heat-treatment processes, when coated on the Sn side of float glass, without the need for any additional surface preparation such as polishing.
- the coating design described in the preceding paragraphs with respect to Example 1 can be applied to the second surface (or Sn side) of the glass to reduce the overall reflection from both interferences.
- Fig. 10 illustrates the light transmission achieved with the above- described design applied to both surfaces of low iron glass before and after tempering/heat-treating.
- the photopic light transmission increases after exposure to a tempering environment and exceeds 99% at normal incidence on 3.2 mm low iron glass.
- Fig. 1 1 illustrates example ranges of physical thicknesses and refractive indices for temperable AR coating 3 when SiOxNy, TiOx, and SiOx are used for the medium index, high index, and low index layers, respectively.
- Figure 9 represents example thicknesses used for each layer in a preferred embodiment of this invention; however, other physical thicknesses may be used for each of the layers in other instances.
- Example ranges for the thicknesses of each layer are as follows:
- SiO x N y (layer 5) 75-135 nm 94-1 15 nm 95 nm
- TiO x (layer 7) 10-35 nm 12-22 nm 21 nm SiO x (layer 9) 70- 130 nm 89-109 nm 105 nm
- AR coatings described herein may be used on thin, low-iron glass.
- Example low-iron glass substrates are disclosed in, for example, U.S. Application Serial No. 12/385,318, as well as in U.S.
- Example 2 was applied to 3.2 mm low-iron glass, the visible transmission was measured at about 99%.
- the coated articles described herein may have a visible transmission of at least about 85%, sometimes at least about 90%, sometimes at least about 95%, and still other times even higher (e.g., around 99%), depending on the desired end-application.
- the following tables show the as coated to heat treated color shifts for the single sided and double sided AR coatings on low-iron glass. It will be appreciated that the heat treatment processes have a reduced (and sometimes no) appreciable impact on the aesthetic (e.g., reflected color) quality of the coating.
- the example coatings described herein have purple hues as deposited, for example. The example purple hue is maintained after heat treatment. This is particularly desirable in a number of applications, where aesthetic quality in terms of reflected color is correspondingly desired.
- the layers described herein may be stoichiometric and/or substantially fully stoichiometric in certain example embodiments; whereas the layers may be sub-stoichiometric in different example embodiments. However, it will be appreciated any suitable stoichiometry may be used in connection with the any of the example layers described herein.
- the layer system or coating is “on” or “supported by” substrate 1 (directly or indirectly), other layer(s) may be provided therebetween.
- the coating 3 of Fig. 1 and the layers thereof may be considered “on” and “supported by” the substrate 1 even if other layer(s) are provided between layer 5 and substrate 1.
- certain layers of the illustrated coating may be removed in certain embodiments, and other layers added in other embodiments of this invention without departing from the overall spirit of certain embodiments of this invention.
- coating 3 may consist essentially of layers 5, 7, and 9, and layer 9 may be exposed to the atmosphere (e.g., layer 9 may be the outermost layer of the coating in certain example embodiments).
- the example embodiments described herein may be used in connection with a variety of applications.
- a single-sided AR coating made according to the example embodiments described herein may be used for applications such as, for example, lights for commercial or residential areas or at sports or other large venues or arenas, lighting application in general, touch screens, etc.
- a double-sided AR coating made according to the example embodiments described herein may be used for applications such as, for example, electronics, displays, appliances, facades, etc.
- other applications also are possible for the example embodiments disclosed herein.
- a coated article as described herein may or may not be heat-treated (e.g., tempered) in certain example embodiments.
- Such tempering and/or heat treatment typically requires use of temperature(s) of at least about 580 degrees C, more preferably of at least about 600 degrees C and still more preferably of at least 620 degrees C.
- the terms "heat treatment” and “heat treating” as used herein mean heating the article to a temperature sufficient to achieve thermal tempering and/or heat strengthening of the glass inclusive article.
- This definition includes, for example, heating a coated article in an oven or furnace at a temperature of at least about 550 degrees C, more preferably at least about 580 degrees C, more preferably at least about 600 degrees C, more preferably at least about 620 degrees C, and most preferably at least about 650 degrees C for a sufficient period to allow tempering and/or heat strengthening. This may be for at least about two minutes, or up to about 10 minutes, in certain example embodiments.
- Some or all of the layers described herein may be disposed, directly or indirectly, on the substrate 1 via sputtering or other suitable film formation technique such as, for example, combustion vapor deposition, combustion deposition, etc.
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- Inorganic Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
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- Organic Chemistry (AREA)
- Surface Treatment Of Glass (AREA)
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- Physical Vapour Deposition (AREA)
- Surface Treatment Of Optical Elements (AREA)
Abstract
Description
Claims
Priority Applications (1)
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PL11728083T PL2611750T3 (en) | 2010-09-03 | 2011-05-24 | Temperable three layer antireflective coating, coated article including temperable three layer antireflective coating, and/or method of making the same |
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US12/923,146 US8693097B2 (en) | 2010-09-03 | 2010-09-03 | Temperable three layer antireflective coating, coated article including temperable three layer antireflective coating, and/or method of making the same |
PCT/US2011/000925 WO2012030372A2 (en) | 2010-09-03 | 2011-05-24 | Temperable three layer antireflective coating, coated article including temperable three layer antireflective coating, and/or method of making the same |
Publications (2)
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EP2611750A2 true EP2611750A2 (en) | 2013-07-10 |
EP2611750B1 EP2611750B1 (en) | 2019-08-28 |
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EP11728083.4A Active EP2611750B1 (en) | 2010-09-03 | 2011-05-24 | Temperable three layer antireflective coating, coated article including temperable three layer antireflective coating, and/or method of making the same |
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US (1) | US8693097B2 (en) |
EP (1) | EP2611750B1 (en) |
JP (1) | JP6043287B2 (en) |
ES (1) | ES2754223T3 (en) |
PL (1) | PL2611750T3 (en) |
TW (1) | TWI624520B (en) |
WO (1) | WO2012030372A2 (en) |
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JP6043287B2 (en) | 2016-12-14 |
EP2611750B1 (en) | 2019-08-28 |
PL2611750T3 (en) | 2020-01-31 |
JP2013542457A (en) | 2013-11-21 |
ES2754223T3 (en) | 2020-04-16 |
TWI624520B (en) | 2018-05-21 |
TW201211175A (en) | 2012-03-16 |
WO2012030372A2 (en) | 2012-03-08 |
US20110157703A1 (en) | 2011-06-30 |
WO2012030372A3 (en) | 2012-06-28 |
US8693097B2 (en) | 2014-04-08 |
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